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60418-63-5

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60418-63-5 Usage

Structure

Pyrazole derivative containing a phenyl group with an azido functional group attached at the 2-position

Usage

Commonly used in organic synthesis, particularly in the preparation of nitrogen-containing heterocycles

Applications

Studied for potential use in medicinal chemistry, specifically in the development of new drugs and pharmaceutical compounds

Importance

Azido group makes it a valuable precursor in the synthesis of various azide-containing compounds for use in chemical biology and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 60418-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,1 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60418-63:
(7*6)+(6*0)+(5*4)+(4*1)+(3*8)+(2*6)+(1*3)=105
105 % 10 = 5
So 60418-63-5 is a valid CAS Registry Number.

60418-63-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-azidophenyl)-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 1-(2-Azidophenyl)pyrazol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:60418-63-5 SDS

60418-63-5Upstream product

60418-63-5Relevant articles and documents

Copper-catalysed regioselective azidation of arenes by C-H activation directed by pyridine

Azad, Chandra S.,Narula, Anudeep K.

, p. 100223 - 100227 (2015/12/04)

A novel and efficient copper-catalysed pyridine directed ortho-azidation of arenes has been developed using safe and stable benzotriazole sulphonyl azide as the azidating agent. A variety of organo azides have been synthesized with electron donor and with

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